Heteroatom containing tetracyclic derivatives as selective estrogen receptor modulators
a technology of estrogen receptor and heteroatom, which is applied in the field of new heteroatoms containing tetracyclic derivatives, can solve the problems of adverse cardiovascular effects, and permanent problems, and achieve the effects of reducing morbidity and mortality among women and men
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example 1
Acetic acid 3-(2,4-dimethoxyphenyl)-7-hydroxy4-methyl-2-oxo-2H-chromen-7-yl ester
[0491]
[0492]A mixture of 2,4-dihydroxyacetophenone (2.233 g, 14.67 mmol, 1 eq), 2, 4-dimethoxyphenylacetic acid (2.88 9, 14.67 mmol, 1 eq), acetic anhydride (7.5 mL, 78 mmol, 5 eq) and triethylamine (1.49 mL, 2.05 mmol, 1 eq) was stirred and heated to reflux under nitrogen for 48 hours. After cooling to room temperature the dark syrupy reaction mixture was poured into ice water (˜450 mL). The suspension of sticky, semisolid product was neutralized by slowly adding solid NaHCO3 to the mixture. The mixture was then allowed to solidify overnight. The dark solid was isolated by filtration, washed with water, sucked dry, and recrystallized from acetic acid to yield the title compound as an ivory crystalline solid. A second crop (0.95 g, 18.3%) was isolated from the mother liquor.
[0493]mp: 146-148° C. MS (Cl) m / z 355 (M+H)+1H NMR (300 MHz, CDCl3): δ 7.67 (1H, d, J=8.7 Hz), 7.13-7.06 (3H, m), 6.58 (1H, d, J=12...
example 2
Acetic acid 3-(2,4-dimethoxyphenyl)-8-hydroxy4-methyl-2-oxo-2H-chromen-7-yl ester
[0494]
[0495]The title compound was prepared according to the procedure described in Example 1 with substitution of 2,3 dihydroxyacetophenone for the 2,4-dihydroxyacetophenone reagent.
[0496]mp 140-141° C. MS (Cl) m / z 355, (M+H)+, 377 (M+Na)+1H NMR (300 MHz, CDCl3): δ 7.55 (1H, d, d, J=4.2, 5.32 Hz), 7.29 (1H, d, J=1.29 Hz), 7.27 (1H, d, J=4.37 Hz), 7.08) 1H, d, J=8.13 Hz), 6.57-6.55 (2H, m), 3.86 (3H, s), 3.76 (3H, s), 2.43 (3H, s), 2.24 (3H, s).
example 3
3-(2,4-Dimethoxyphenyl)-7-fluoro-4-methyl-2-oxo-2H-chromen-7-yl ester
[0497]
[0498]The title compound was prepared according to the procedure described in Example 1 with substitution of 4-fluoro-2-hydroxyacetophenone for the 2,4-dihydroxyacetophenone reagent.
[0499]mp 156-157° C. MS (Cl) m / z 315 (M+H)+, 337 (M+Na)+1H NMR (300 MHz, CDCl3): δ 7.64 (1H, d, d, J=5.98, 8.77 Hz), 7.11-7.01 (3H, m), 6.58 (1H, d, d, J=2.30, 8.10 Hz), 6.57 (1H, s), 3.86 (3H, s), 3.77 (3H, s), 2.24 (3H, s) IR (KBr): 1712, 1617, 1527, 1505, 1215, 1118 cm−1 Anal. Calc. C18H15O4: C, 68.78; H, 4.84. Found: C, 68.67; H, 4.70.
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